Phung Abraham T, Shah Jaimin R, Dong Tao, Aisagbonhi Omonigho, Trogler William C, Kummel Andrew C, Blair Sarah L
Moores Cancer Center, University of California San Diego, San Diego, CA 92037, USA.
Department of Chemistry and Biochemistry, University of California San Diego, San Diego, CA 92037, USA.
Pharmaceutics. 2025 Jun 11;17(6):769. doi: 10.3390/pharmaceutics17060769.
: While adenovirus (Ad) therapies have been proven to be effective in local administration, systemic Ad treatments have shown limited success due to pre-existing antibodies in the human blood that neutralize the virus. We developed a liposome coating procedure that protects the Ad from pre-existing neutralizing antibodies in human blood. To assess the in vivo stability of the liposomes, the present study used a novel in vivo method to quantitatively assess the protective capabilities of liposome-encapsulated Ad (DfAd) from neutralizing antibodies. : The assay systemically administers DfAd with a green fluorescent protein transgene (DfAd-GFP) into pre-immunized mice and allows it to circulate in the presence of neutralizing antibodies; the infected blood is extracted and used to transduce HEK293 cells, which emits fluorescence in the presence of protected, un-neutralized Ad. : The PEGylated liposome formulation provides 12× protection in vivo relative to unencapsulated Ads. In vitro optimization of the liposome coating reveals a strong correlation between the structural stability of liposomes and protection against anti-Ad neutralizing antibodies, where DSPE-PEG2000-carboxylic acid (DSPE-PEG2000-CA) is a critical component for liposome stability and increasing protection against antibody neutralization of the encapsulated Ad. : The findings in the present study confirm that the DfAd liposome can protect against neutralizing antibodies in blood circulation. The novel in vivo assay for liposome protection against neutralizing antibodies and in vitro experiments in the present study provide new tools and insights toward designing liposome-Ad complexes for the systemic treatment of cancer.
虽然腺病毒(Ad)疗法已被证明在局部给药中有效,但由于人类血液中预先存在的中和病毒的抗体,全身性Ad治疗的成功率有限。我们开发了一种脂质体包被程序,可保护Ad免受人类血液中预先存在的中和抗体的影响。为了评估脂质体在体内的稳定性,本研究使用了一种新型的体内方法来定量评估脂质体包裹的Ad(DfAd)免受中和抗体的保护能力。该检测系统将携带绿色荧光蛋白转基因的DfAd(DfAd-GFP)全身给药到预先免疫的小鼠体内,并使其在中和抗体存在的情况下循环;提取感染的血液并用于转导HEK293细胞,在存在受保护的、未被中和的Ad时,HEK293细胞会发出荧光。聚乙二醇化脂质体制剂在体内相对于未包封的Ad提供了12倍的保护。脂质体包被的体外优化揭示了脂质体的结构稳定性与抗Ad中和抗体保护之间的强相关性,其中1,2-二硬脂酰-sn-甘油-3-磷酸乙醇胺-N-[甲氧基(聚乙二醇)-2000]-羧酸(DSPE-PEG2000-CA)是脂质体稳定性和增强对包封Ad抗体中和保护的关键成分。本研究的结果证实,DfAd脂质体可以保护免受血液循环中的中和抗体的影响。本研究中针对脂质体免受中和抗体保护的新型体内检测和体外实验为设计用于癌症全身治疗的脂质体-Ad复合物提供了新工具和见解。